All Stories

  1. The World Health Organisation's list of essential medicines and haemophilia treatment products
  2. In response: Overestimation of fibrinogen concentration in cryoprecipitate by repeated freeze–thawing with long thawing period as used in the Clauss method
  3. The Evolution of the Safety of Plasma Products from Pathogen Transmission—A Continuing Narrative
  4. The best use of the French donors’ gift – Continuing an ethical tradition
  5. The legacy of haemophilia: Memories and reflections from three survivors
  6. Therapeutic Solutions of Human Albumin – The Possible Effect of Process-Induced Molecular Alterations on Clinical Efficacy and Safety
  7. Fresh frozen plasma: Beyond coagulation factor content
  8. Albumin in plasma exchange – A rethink is required
  9. Storage of cryoprecipitate: Role of blood storage
  10. The safety of plasma‐derived haemophilia factor concentrates – comments on “Deep viral metagenomics in patients with haemophilia receiving plasma‐derived coagulation factor concentrates” Nunes Valença I et al. (2021). Deep viral metagenomics in patient...
  11. The discovery of cryoprecipitate as a modality for hemophilia A: Augmenting the allocation of credit
  12. Appropriately specifying the quality of plasma for fractionation
  13. Estimation of the latent therapeutic demand for immunoglobulin therapies in autoimmune neuropathies in the United States
  14. Is plasma donation ethics abused?
  15. The interphase between immunoglobulin, the plasma industry and the public health, managing a finite resource
  16. The art of the possible in approaching efficacy trials for COVID19 convalescent plasma
  17. Intravenous Immunoglobulin Rich in Neutralising Antibodies to SARS-CoV-2 as a Passive Immunity Modality in Healthy Individuals at Risk of Infection With COVID-19: Study Protocol for an Open Label, Active Control Phase 1/2 Study.
  18. Urgent Need to Regulate Convalescent Plasma Differently from Thawed Plasma
  19. ABO‐incompatible convalescent plasma transfusion: Yes, you can
  20. Supporting Garraud – and protecting transfusion
  21. Plasma from donors convalescent from SARS-CoV-2 infection–A matter of priorities
  22. Convalescent plasma – this is no time for competition
  23. Latent Therapeutic Demand of Immunoglobulin therapies in neuropathies in the United States
  24. The impact of the SARS-CoV-2 outbreak on the safety and availability of blood transfusions in Italy
  25. Concerns regarding immunoglobulins
  26. Pharmacokinetics of a new human plasma‐derived double virus inactivated and nanofiltered factor IX concentrate in previously treated severe or moderately severe haemophilia B patients
  27. Pharmacokinetic and safety considerations when switching from standard to extended half-life clotting factor concentrates in hemophilia
  28. Comparing objective and self‐reported measures of adherence in haemophilia
  29. Herd immunity and primary immune deficiencies
  30. Health-Related Quality of Life in Patients with CVID Under Different Schedules of Immunoglobulin Administration: Prospective Multicenter Study
  31. Comparative analysis of marketed factor VIII products: comment
  32. The burden of common variable immunodeficiency disorders: a retrospective analysis of the European Society for Immunodeficiency (ESID) registry data
  33. Improving access to haemophilia therapies-Beyond humanitarian aid
  34. Perspectives on haemophilia access in Brazil?
  35. The multiple benefits of sport in haemophilia
  36. Factor VIII manufactured from plasma—the ups and downs, and the up again: a personal journey—part 1: history of the development of plasma-derived factor VIII therapies
  37. Factor VIII manufactured from plasma—the ups and downs, and the up again: a personal journey—part 2: aspects of factor VIII manufacture from plasma
  38. Obituary: Duncan Stephen Pepper, 1942-2017
  39. Concerns regarding clinical trials in haemophilia-Augmenting Iorio's “Research and policy implications of a recently published controlled study in previously untreated haemophilia patients at high risk of inhibitor development” Haemophilia (2017), 1-3 htt
  40. Time to review the way we estimate access to haemophilia concentrates worldwide
  41. The dynamics of contract plasma fractionation
  42. Usual and unusual mutations in a cohort of Belgian patients with hemophilia B
  43. Innovation in Hemophilia Therapies — “And Miles to Go, before [We] Sleep”
  44. Are we optimising outcomes in Australia’s framework for the supply of plasma-derived medicines?
  45. Safety Issues of Plasma-Derived Products for Treatment of Inherited Bleeding Disorders
  46. Where now for transfusion: the evolution of a paradigm and its logical progression
  47. Editorial: Immunoglobulin Therapy in the 21st Century – the Dark Side of the Moon
  48. Ethical issues in clinical trials
  49. Assessing options for treating haemophilia with inhibitors
  50. Errors and Omissions: Donor Compensation Policies and Richard Titmuss
  51. Reflections on the emergence of chikungunya virus in the United States: time to revisit a successful paradigm for the safety of blood-derived therapies
  52. Estimation of the latent therapeutic demand for albumin in the USA: a focus on three indications
  53. Use of albumin in spontaneous bacterial peritonitis is cost-effective
  54. Manufacture of Immunoglobulin Products for Patients with Primary Antibody Deficiencies – The Effect of Processing Conditions on Product Safety and Efficacy
  55. Hemolysis in patients with antibody deficiencies on immunoglobulin replacement treatment
  56. The Ethics of Paid Plasma Donation: A Plea for Patient Centeredness
  57. Choice of Fluids in Severe Septic Patients - A Cost-effectiveness Analysis Informed by Recent Clinical Trials
  58. Joint WFH-ISTH session: issues in clinical trial design
  59. Products Used to Treat Hemophilia: Regulation
  60. Hemophilia treatment and the AIDS tragedy: closing the circle
  61. Toward a patient-based paradigm for blood transfusion
  62. Clinical Trial Design for Alpha-1 Antitrypsin Deficiency: A Model for Rare Diseases
  63. Modeling Primary Immunodeficiency Disease Epidemiology and Its Treatment to Estimate Latent Therapeutic Demand for Immunoglobulin
  64. Relative Survival Benefit and Morbidity with Fluids in Severe Sepsis - A Network Meta-Analysis of Alternative Therapies
  65. Treatment for life for severe haemophilia A- A cost-utility model for prophylaxis vs. on-demand treatment
  66. Economic considerations on transfusion medicine and patient blood management
  67. External Financial Aid to Blood Transfusion Services in Sub-Saharan Africa: A Need for Reflection
  68. The Boldt Affair
  69. Assessing causality in the transmission of viruses by blood products
  70. Albumin from rice: Why and wherefore?
  71. Health technology assessment and haemophilia
  72. Letter to the Editor - Response to ‘How expanding voluntary non-remunerated blood donations would benefit patients, donors and healthcare systems?’- F. Rossi, R. Perry, J. de Wit,T. Evers & G. Folléa, Vox Sanguinis DOI: 10.1111/j.1423-0410.2011.01495.x
  73. Conditions for plasma processing
  74. Response to Laub et al., ‘Specific protein content of pools of plasma for fractionation from different sources: impact of frequency of donations’, Vox Sanguinis (2010) 99, 220-231
  75. Safety of Plasma Volume Expanders
  76. A study of reported factor IX use around the world
  77. HIV safety in sub-Saharan Africa
  78. Response to Volkow P et al. – Cross-border paid plasma donation among injection drug users in two Mexico–U.S. border cities – International Journal of Drug Policy 20 (2009) 409–412
  79. Falsification or paradigm shift? Toward a revision of the common sense of transfusion
  80. Products used to Treat Hemophilia: Regulation
  81. Payment, compensation and replacement - the ethics and motivation of blood and plasma donation
  82. Albumin Usage in Clinical Medicine: Tradition or Therapeutic?
  83. Concerning Chapter 5 – Human Albumin; in Cross-Sectional Guidelines for Therapy with Blood Components and Plasma Derivatives, 4th ed. Transfus Med Hemother 2009;36(6):399–407
  84. A study of reported factor VIII use around the world
  85. Globalisation and blood safety
  86. Remuneration of blood donors: let us compare apples with apples
  87. Plasma fractionation issues
  88. Stem cell and cellular therapy developments
  89. Trialing plasma protein therapies for rare disorders: Thinking outside the box
  90. Comparison of the risk of viral infection between the living and nonliving musculoskeletal tissue donors in Australia
  91. Trends in Prevalence of Viral Infections in Australian Musculoskeletal Tissue Donors and Projections of Incidence and Residual Risk, 1993–2004
  92. Platelet size analysis in the quality assurance of platelet concentrates for transfusion
  93. Reply
  94. The Risk of HIV, HBV, HCV and HTLV Infection Among Musculoskeletal Tissue Donors in Australia
  95. Theoretically estimated risk of severe acute respiratory syndrome transmission through blood transfusion during an epidemic in Shenzhen, Guangdong, China in 2003
  96. Residual risk of transfusion-transmitted viral infections in Shenzhen, China, 2001 through 2004
  97. Global Forum of the World Federation of Hemophilia, September 26–27, 2005, Montreal, Quebec, Canada
  98. CHALLENGES IN THE EVALUATION OF SAFETY AND EFFICACY OF HUMAN TISSUE AND CELL BASED PRODUCTS
  99. When do tissues and cells become products? – Regulatory oversight of emerging biological therapies
  100. Plasma protein therapies: current and future perspectives
  101. Assessing Efficacy and Therapeutic Claims in Emerging Indications for Recombinant Factor VIIa: Regulatory Perspectives
  102. Variant Creutzfeldt-Jakob disease transmission by plasma products: assessing and communicating risk in an era of scientific uncertainty
  103. Choice of replacement therapy for hemophilia-cryoprecipitate issues: a rebuttal
  104. The mantra of blood safety: time for a new tune?
  105. The Cambridge Healthtech Institute’s 9th Annual Conference on Blood Safety
  106. Risk of parvovirus infection by immunoglobulin
  107. Modulation of fibrinogen content in cryoprecipitate by temperature manipulation during plasma processing
  108. The Cambridge Healthtech Institute?s 9th Annual Conference on Blood Safety
  109. The regulatory pendulum in transfusion medicine
  110. Evolving perspectives in product safety for haemophilia
  111. Haemophilia 2002: emerging risks of treatment
  112. Risk of variant Creuzfeldt-Jakob disease from factor concentrates: current perspectives
  113. Laboratory practice and studies of bovine spongiform encephalopathy
  114. Intravenous immunoglobulin: regulatory perspectives on use and supply
  115. Flow–Cytometric Method for the Quantitation of the Fc Function of Intravenous Immunoglobulin Preparations
  116. Biological Activity of von Willebrand factor during the manufacture of therapeutic factor VIII concentrates as determined by the collagen-binding assay
  117. Measurement of Anticomplementary Activity in Therapeutic Intravenous Immunoglobulin Preparations
  118. Hepatitis C virus transmission by intravenous immunoglobulin
  119. Relative Efficiency of Leucocyte Removal Procedures for the Production of Leucocyte-Poor Red Cell Concentrates Assessed by Flow Cytometry
  120. In vitro properties of additive suspended red cells collected into a dextrose-free anticoagulant
  121. Platelet Concentrates for Transfusion—Metabolic and Storage Aspects
  122. Components prepared from blood collected into dextrose-free anticoagulant. In vitro properties of platelets suspended in plasma and in dextrose-free synthetic medium
  123. Storage of platelet concentrates harvested from blood collected into dextrose-free preservative without agitation
  124. Cryopreservation of red blood cells: effect of freezing on red cell quality and residual lymphocyte immunogenicity.
  125. Stablization of von Willebrand factor in banked blood by leucocyte depletion
  126. Factor VIII/von willebrand factor levels in plasma frozen to - 30 ° C in air or halogenated hydrocarbons
  127. Red Cell and Platelet Concentrates from Blood Collected into Half-Strength Citrate Anticoagulant: Improved Maintenance of Red Cell 2,3-Diphosphoglycerate in Half-Citrate Red Cells
  128. Von Willebrand factor characterization of a severe dry-heat treated factor VIII concentrate, AHF (high purity)
  129. Improved in-vitro quality of platelet concentrates stored in a dextrose-free synthetic medium
  130. Viral safety of coagulation factor concentrates
  131. Microtitre plate measurement of platelet response to hypotonic stress.
  132. Effects of Plasma Collection Systems and Processing Parameters on the Quality of Factor IX Concentrate
  133. A microtitre plate test for assesment of in-vitro thrombogenicity in factor IX concentrates using a chromogenic substrate
  134. Studies on the Procurement of Blood Coagulation Factor VIII in vitro Studies on Blood Components Prepared in Half-Strength Citrate Anticoagulant
  135. Donation Procedure, Fibrinopeptide A, and Factor VIII
  136. Products Used to Treat Hemophilia: Regulation